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Quality Engineer Process Engineer Jobs in Maine (NOW HIRING)

Assists materials, process, manufacturing, and quality engineers to solve processing and procedural issues, and create component fixtures and tooling solutions * Develops, implements, and sustains ...

Lead and execute advanced quality engineering activities including process validation, risk assessments, and supplier quality improvements. * Oversee CAPAs, complaints, and audit follow-up activities ...

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Quality Engineer Process Engineer information

See Maine salary details

$33.4K

$83.2K

$116.7K

How much do quality engineer process engineer jobs pay per year?

As of Jun 14, 2026, the average yearly pay for quality engineer process engineer in Maine is $83,216.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,600.00 and $95,900.00 per year, depending on experience, location, and employer.

Are quality engineer and process engineer the same?

A quality engineer focuses on ensuring products meet quality standards through inspections, testing, and process improvements, often using tools like Six Sigma. A process engineer designs, implements, and optimizes manufacturing or operational processes to improve efficiency and reduce costs. While both roles aim to improve product and process quality, they have different primary responsibilities and skill sets.

What is the difference between Quality Engineer Process Engineer vs Quality Engineer?

AspectQuality EngineerProcess Engineer
Primary FocusQuality assurance, defect prevention, complianceProcess improvement, efficiency, workflow optimization
CertificationsASQ CQE, ISO auditorSix Sigma, Lean certifications
Work EnvironmentManufacturing, production, quality labsManufacturing, engineering, production lines
Common Industry UsageQuality control departmentsProcess improvement teams

While both roles are vital in manufacturing, a Quality Engineer primarily focuses on ensuring product quality and compliance, whereas a Process Engineer concentrates on optimizing manufacturing processes for efficiency. Understanding these differences helps employers and professionals align skills with job requirements effectively.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as petroleum engineering, software engineering, and aerospace engineering can earn $300,000 or more annually, especially with extensive experience, advanced skills, and leadership roles. High-level process or quality engineers in certain industries or companies may also reach this salary level, often requiring advanced certifications and expertise in their domain.

What engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, especially with experience, advanced skills, and bonuses. High-level roles often require advanced degrees, certifications, and leadership responsibilities within their organizations.

What does a process quality engineer do?

A process quality engineer is responsible for developing, implementing, and maintaining manufacturing processes to ensure product quality and efficiency. They analyze data, perform root cause analysis, and use tools like Six Sigma or statistical process control to identify and resolve process issues, often working closely with production teams. Certification in quality management systems and strong analytical skills are typically required for this role.
What cities in Maine are hiring for Quality Engineer Process Engineer jobs? Cities in Maine with the most Quality Engineer Process Engineer job openings:

Associate Manufacturing Line Quality Engineer

Abbott

Scarborough, ME • On-site

$50K - $101K/yr

Full-time

Medical, Life, Retirement

Posted 13 days ago


Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

146th of 518 rated manufacturers


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

Associate Manufacturing Line Quality Engineer (2nd Shift Position)

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution.

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
This position works out of our Scarborough, ME location in the Infectious Disease, Diagnostics Division. We're empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott's diagnostics instruments, providing lab results for millions of people.

The Associate Manufacturing Line Quality Engineer (2nd shift position) is within our Infectious Disease business unit located at all sites under Abbott Diagnostics Scarborough Quality Management System (QMS). In this role you will provide support for product quality assurance, process improvements, and all quality system programs.

Working Hours: 2nd Shift Monday - Friday, 2:00 pm - 10:30 pm

What You'll Work On

  • Support production with resolution of quality issues in accordance with established procedures.

  • Support production on the manufacturing floor, ensuring adherence to procedures and ensuring appropriate device history record (DHR) documentation. Supports line clearances, reworks, and inspections as required.

  • Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.

  • Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.

  • Understands and is aware of the quality consequences which may result from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.

  • Other duties as assigned, according to the changing needs of the business.

Required Qualifications

  • Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life Science or other technical field or the equivalent Combination of education and experience.

Preferred Qualifications

  • Working knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.

  • Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements

  • Strong technical writing skills and effective communication skills.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

The base pay for this position is

$50,700.00 - $101,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Operations QualityDIVISION:ID Infectious DiseaseLOCATION:United States > Scarborough : 10 Southgate RdADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 5 % of the TimeMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Work in noisy environment, Work requiring repeated bending, stooping, squatting or kneelingAbbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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